264 related articles for article (PubMed ID: 28903150)
1. Crx-L253X Mutation Produces Dominant Photoreceptor Defects in TVRM65 Mice.
Ruzycki PA; Linne CD; Hennig AK; Chen S
Invest Ophthalmol Vis Sci; 2017 Sep; 58(11):4644-4653. PubMed ID: 28903150
[TBL] [Abstract][Full Text] [Related]
2. Mechanistically distinct mouse models for CRX-associated retinopathy.
Tran NM; Zhang A; Zhang X; Huecker JB; Hennig AK; Chen S
PLoS Genet; 2014 Feb; 10(2):e1004111. PubMed ID: 24516401
[TBL] [Abstract][Full Text] [Related]
3. Graded gene expression changes determine phenotype severity in mouse models of CRX-associated retinopathies.
Ruzycki PA; Tran NM; Kefalov VJ; Kolesnikov AV; Chen S
Genome Biol; 2015 Sep; 16(1):171. PubMed ID: 26324254
[TBL] [Abstract][Full Text] [Related]
4. CrxRdy Cat: A Large Animal Model for CRX-Associated Leber Congenital Amaurosis.
Occelli LM; Tran NM; Narfström K; Chen S; Petersen-Jones SM
Invest Ophthalmol Vis Sci; 2016 Jul; 57(8):3780-92. PubMed ID: 27427859
[TBL] [Abstract][Full Text] [Related]
5. Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.
Jacobson SG; Cideciyan AV; Huang Y; Hanna DB; Freund CL; Affatigato LM; Carr RE; Zack DJ; Stone EM; McInnes RR
Invest Ophthalmol Vis Sci; 1998 Nov; 39(12):2417-26. PubMed ID: 9804150
[TBL] [Abstract][Full Text] [Related]
6. OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness.
Roger JE; Hiriyanna A; Gotoh N; Hao H; Cheng DF; Ratnapriya R; Kautzmann MA; Chang B; Swaroop A
J Clin Invest; 2014 Feb; 124(2):631-43. PubMed ID: 24382353
[TBL] [Abstract][Full Text] [Related]
7. Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy.
Itabashi T; Wada Y; Sato H; Kawamura M; Shiono T; Tamai M
Am J Ophthalmol; 2004 Nov; 138(5):876-7. PubMed ID: 15531334
[TBL] [Abstract][Full Text] [Related]
8. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM
Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607
[TBL] [Abstract][Full Text] [Related]
9. Delayed expression of the Crx gene and photoreceptor development in the Chx10-deficient retina.
Rutherford AD; Dhomen N; Smith HK; Sowden JC
Invest Ophthalmol Vis Sci; 2004 Feb; 45(2):375-84. PubMed ID: 14744875
[TBL] [Abstract][Full Text] [Related]
10. Different effects of valproic acid on photoreceptor loss in Rd1 and Rd10 retinal degeneration mice.
Mitton KP; Guzman AE; Deshpande M; Byrd D; DeLooff C; Mkoyan K; Zlojutro P; Wallace A; Metcalf B; Laux K; Sotzen J; Tran T
Mol Vis; 2014; 20():1527-44. PubMed ID: 25489226
[TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene.
Tzekov RT; Liu Y; Sohocki MM; Zack DJ; Daiger SP; Heckenlively JR; Birch DG
Invest Ophthalmol Vis Sci; 2001 May; 42(6):1319-27. PubMed ID: 11328746
[TBL] [Abstract][Full Text] [Related]
12. Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog.
Akhmedov NB; Baldwin VJ; Zangerl B; Kijas JW; Hunter L; Minoofar KD; Mellersh C; Ostrander EA; Acland GM; Farber DB; Aguirre GD
Mol Vis; 2002 Mar; 8():79-84. PubMed ID: 11951083
[TBL] [Abstract][Full Text] [Related]
13. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
Freund CL; Gregory-Evans CY; Furukawa T; Papaioannou M; Looser J; Ploder L; Bellingham J; Ng D; Herbrick JA; Duncan A; Scherer SW; Tsui LC; Loutradis-Anagnostou A; Jacobson SG; Cepko CL; Bhattacharya SS; McInnes RR
Cell; 1997 Nov; 91(4):543-53. PubMed ID: 9390563
[TBL] [Abstract][Full Text] [Related]
14. Retinopathy and attenuated circadian entrainment in Crx-deficient mice.
Furukawa T; Morrow EM; Li T; Davis FC; Cepko CL
Nat Genet; 1999 Dec; 23(4):466-70. PubMed ID: 10581037
[TBL] [Abstract][Full Text] [Related]
15. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Pang JJ; Chang B; Hawes NL; Hurd RE; Davisson MT; Li J; Noorwez SM; Malhotra R; McDowell JH; Kaushal S; Hauswirth WW; Nusinowitz S; Thompson DA; Heckenlively JR
Mol Vis; 2005 Feb; 11():152-62. PubMed ID: 15765048
[TBL] [Abstract][Full Text] [Related]
16. Mechanisms of blindness: animal models provide insight into distinct CRX-associated retinopathies.
Tran NM; Chen S
Dev Dyn; 2014 Oct; 243(10):1153-66. PubMed ID: 24888636
[TBL] [Abstract][Full Text] [Related]
17. The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes.
Peng GH; Ahmad O; Ahmad F; Liu J; Chen S
Hum Mol Genet; 2005 Mar; 14(6):747-64. PubMed ID: 15689355
[TBL] [Abstract][Full Text] [Related]
18. Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy.
Chen S; Wang QL; Xu S; Liu I; Li LY; Wang Y; Zack DJ
Hum Mol Genet; 2002 Apr; 11(8):873-84. PubMed ID: 11971869
[TBL] [Abstract][Full Text] [Related]
19. Induction of functional photoreceptor phenotype by exogenous Crx expression in mouse retinal stem cells.
Jomary C; Jones SE
Invest Ophthalmol Vis Sci; 2008 Jan; 49(1):429-37. PubMed ID: 18172122
[TBL] [Abstract][Full Text] [Related]
20. Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.
Ishiba Y; Higashide T; Mori N; Kobayashi A; Kubota S; McLaren MJ; Satoh H; Wong F; Inana G
Exp Eye Res; 2007 Mar; 84(3):473-85. PubMed ID: 17174953
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
